@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP182609.RAfsfrrLQPcYvett3OggVNo_tQnU4S9zGmRw2BEBLJHYg
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP182609.RAfsfrrLQPcYvett3OggVNo_tQnU4S9zGmRw2BEBLJHYg130_head
{
this:
np:hasAssertion
dgn-np:NP182609.RAfsfrrLQPcYvett3OggVNo_tQnU4S9zGmRw2BEBLJHYg130_assertion
;
np:hasProvenance
dgn-np:NP182609.RAfsfrrLQPcYvett3OggVNo_tQnU4S9zGmRw2BEBLJHYg130_provenance
;
np:hasPublicationInfo
dgn-np:NP182609.RAfsfrrLQPcYvett3OggVNo_tQnU4S9zGmRw2BEBLJHYg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP182609.RAfsfrrLQPcYvett3OggVNo_tQnU4S9zGmRw2BEBLJHYg130_assertion
a
np:Assertion
.
dgn-np:NP182609.RAfsfrrLQPcYvett3OggVNo_tQnU4S9zGmRw2BEBLJHYg130_provenance
a
np:Provenance
.
dgn-np:NP182609.RAfsfrrLQPcYvett3OggVNo_tQnU4S9zGmRw2BEBLJHYg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP182609.RAfsfrrLQPcYvett3OggVNo_tQnU4S9zGmRw2BEBLJHYg130_assertion
{
miriam-gene:1636
a
ncit:C16612
.
lld:C0038454
a
ncit:C7057
.
dgn-gda:DGN0d5fb5a6b02c6cded1f1882caf426bd2
sio:SIO_000628
miriam-gene:1636
,
lld:C0038454
;
a
sio:SIO_001121
.
}
dgn-np:NP182609.RAfsfrrLQPcYvett3OggVNo_tQnU4S9zGmRw2BEBLJHYg130_provenance
{
dgn-np:NP182609.RAfsfrrLQPcYvett3OggVNo_tQnU4S9zGmRw2BEBLJHYg130_assertion
dcterms:description
"[Linkage analyses in experimental crosses of stroke-prone spontaneously hypertensive (SHRSP) and normotensive Wistar-Kyoto (WKY) rats have strongly suggested the presence of quantitative trait loci (QTL) influencing blood pressure and ACE levels on rat chromosome 10, which have been confirmed in multiple independent studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:12642508
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP182609.RAfsfrrLQPcYvett3OggVNo_tQnU4S9zGmRw2BEBLJHYg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:39+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}